Entry Level Medical Device Hardware Test Engineer

Our client, a medical device technology organization, is seeking an Entry Level Medical Device Hardware Test Engineer to join their team. As an Entry Level Medical Device Hardware Test Engineer, you will be part of the engineering organization supporting verification and validation activities. The ideal candidate will have strong attention to detail, hands-on laboratory testing experience, and clear technical communication skills, which will align successfully in the organization. Job Title: Entry Level Medical Device Hardware Test Engineer Location: Saint Paul, Minnesota (Onsite) Pay Range: $30/hr. ON W2 What's the Job?

• Execute board-level and system-level verification testing in accordance with approved protocols and procedures.
• Review and interpret product requirements, electrical schematics, engineering documentation, and test procedures.
• Configure and execute laboratory test setups using standard electrical test equipment.
• Perform electrical measurements, collect test data, and document results accurately and traceably.
• Investigate, troubleshoot, and document test failures, anomalies, and observations while supporting design verification and validation. What's Needed?
• BS or MS in Electrical Engineering, Electronics Engineering, ECE, EEE, or a related field (recent graduates with relevant internships, laboratory, or project experience are encouraged).
• Strong foundation in analog and digital electronics.
• Ability to read and understand electrical schematics, engineering drawings, and test protocols.
• Hands-on experience with laboratory equipment such as oscilloscopes, multimeters, power supplies, signal generators, and logic analyzers.
• Strong technical documentation skills, including creation of test records, execution reports, and defect documentation, plus effective written and verbal communication. What's in it for me?
• Work onsite in Saint Paul, Minnesota, supporting medical device hardware quality through hands-on testing.
• Build real-world experience executing verification and validation activities for regulated medical device products.
• Collaborate with cross-functional engineering teams including Electrical, Firmware, Mechanical, Systems, Quality, and Regulatory Engineering.
• Develop stronger troubleshooting and problem-solving skills by investigating test failures and anomalies.
• Contribute to clear, traceable documentation that supports compliance and product reliability. If this is a role that interests you and you'd like to learn more, click apply now and a recruiter will be in touch with you to discuss this great opportunity. We look forward to speaking with you! About ManpowerGroup, Parent Company of: Manpower, Experis, Talent Solutions, and Jefferson Wells. ManpowerGroup® (NYSE: MAN), the leading global workforce solutions company, helps organizations transform in a fast-changing world of work by sourcing, assessing, developing, and managing the talent that enables them to win. We develop innovative solutions for hundreds of thousands of organizations every year, providing them with skilled talent while finding meaningful, sustainable employment for millions of people across a wide range of industries and skills. Our expert family of brands – Manpower, Experis, Talent Solutions, and Jefferson Wells – creates substantial value for candidates and clients across more than 75 countries and territories and has done so for over 70 years. We are recognized consistently for our diversity - as a best place to work for Women, Inclusion, Equality and Disability and in 2023 ManpowerGroup was named one of the World's Most Ethical Companies for the 14th year - all confirming our position as the brand of choice for in-demand talent.